Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methacrylic Acid | HCID 4093 | — |
| Reactant | 4-Hydroxybenzophenone | HCID 14347 | — |
| Reactant | Tetrabutylammonium Hydroxide | HCID 2723671 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | Benzophenone | HCID 3102 | — |
| Product | Methacrylate | HCID 87595 | — |
Reaction Steps
In the following example, a terpolymer derivative having 0.88 mole % methacrylate and 0.07 mole % benzophenone (graft ratio 92.7%:7.3% methacrylate:benzophenone) was prepared by a procedure to Example A-3 except that the tetrabutylammonium salt was prepared by charging 101.3 mL tetrabutylammonium hydroxide (1.0 M in methanol), 8.3 g (8.2 mL) methacrylic acid, 1.01 g 4-hydroxybenzophenone, and 100 mL isopropanol to a second flask and stirring at room temperature to give a translucent yellowish solution. This mixture was then added to the polymeric cement, as in Example 4. The polymer was isolated by precipitation in isopropanol with 0.1% BHT stabilizer optionally added. 1HNMR (400 MHz, CDCl3) analysis confirmed 97.3% conversion of benzylic bromide to grafted species. These results are given in Table A.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05459174 |
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| Source dataset | uspto-grants-1995_10 |
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| ORD ID | ord-73f4fa953e8c490a85e2ecc50c7c54b2 |
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| Source note | uspto-grants-1995_10 |
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